NDC 57842-7732 Doctorrelief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57842-7732?
What are the uses for Doctorrelief?
Which are Doctorrelief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Doctorrelief Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- TRICHOSANTHES CUCUMERINA SEED (UNII: O6375G869C)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- PHELLODENDRON CHINENSIS BARK (UNII: 2866QMZ434)
- TURMERIC (UNII: 856YO1Z64F)
- ARISAEMA ERUBESCENS ROOT (UNII: 3E8P1PU8SY)
- GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- TANGERINE (UNII: KH3E3096OO)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- SESAME OIL (UNII: QX10HYY4QV)
What is the NDC to RxNorm Crosswalk for Doctorrelief?
- RxCUI: 1111030 - camphor 2.25 % / menthol 7.5 % / methyl salicylate 3.75 % Medicated Patch
- RxCUI: 1111030 - camphor 0.0225 MG/MG / menthol 0.075 MG/MG / methyl salicylate 0.0375 MG/MG Medicated Patch
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".